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B Eng

Showing results (71-80 of 99) with videos related to

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American Journal of Hematology|September 1, 1994
DNA diagnosis of Hb S and Hb Caribbean (alpha 2 beta 2 91 Leu-->Arg) in a Jamaican familyJ S Waye, M Patterson, B Eng, et al.
Hemoglobin|October 10, 1997
Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H diseaseJ S Waye, B Eng, M Patterson, et al.
Journal of Drugs in Dermatology : JDD|July 8, 2017
Prospective Study of Pathogenesis of Atrophic Acne Scars and Role of Macular ErythemaJerry Tan, Valérie Bourdès, Robert Bissonnette, et al.
American Journal of Hematology|January 1, 1991
Antithrombin III-Amiens: a new family with an Arg47----Cys inherited variant of antithrombin III with impaired heparin cofactor activityB Roussel, J Dieval, J Delobel, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1993
Carrier detection and prenatal diagnosis of hemoglobinopathies in OntarioJ S Waye, B Eng, S P Cai, et al.
Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.
Blood|March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemiaW Tang, S P Cai, B Eng, et al.
Thrombosis Research|May 1, 1994
Characterization of a highly polymorphic trinucleotide short tandem repeat within the human antithrombin geneH Ni, J S Waye, R C Austin, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Hematology|September 18, 2001
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 casesJ S Waye, B Eng, M Patterson, et al.
Pageof 10

Showing results (71-80 of 99) with videos related to

Sort By:
Pageof 10
American Journal of Hematology|September 1, 1994
DNA diagnosis of Hb S and Hb Caribbean (alpha 2 beta 2 91 Leu-->Arg) in a Jamaican familyJ S Waye, M Patterson, B Eng, et al.
Hemoglobin|October 10, 1997
Novel mutation of the alpha 2-globin gene initiation codon (ATG-->A-G) in a Vietnamese girl with Hb H diseaseJ S Waye, B Eng, M Patterson, et al.
Journal of Drugs in Dermatology : JDD|July 8, 2017
Prospective Study of Pathogenesis of Atrophic Acne Scars and Role of Macular ErythemaJerry Tan, Valérie Bourdès, Robert Bissonnette, et al.
American Journal of Hematology|January 1, 1991
Antithrombin III-Amiens: a new family with an Arg47----Cys inherited variant of antithrombin III with impaired heparin cofactor activityB Roussel, J Dieval, J Delobel, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|October 1, 1993
Carrier detection and prenatal diagnosis of hemoglobinopathies in OntarioJ S Waye, B Eng, S P Cai, et al.
Hemoglobin|January 17, 2002
Identification of two new alpha-thalassemia mutations in exon 2 of the alpha1-globin geneJ S Waye, B Eng, M Patterson, et al.
Blood|March 15, 1993
Expression of embryonic zeta-globin and epsilon-globin chains in a 10-year-old girl with congenital anemiaW Tang, S P Cai, B Eng, et al.
Thrombosis Research|May 1, 1994
Characterization of a highly polymorphic trinucleotide short tandem repeat within the human antithrombin geneH Ni, J S Waye, R C Austin, et al.
Journal of Medical Genetics|June 19, 2002
Smith-Lemli-Opitz syndrome: carrier frequency and spectrum of DHCR7 mutations in CanadaJ S Waye, L M Nakamura, B Eng, et al.
American Journal of Hematology|September 18, 2001
Hemoglobin H (Hb H) disease in Canada: molecular diagnosis and review of 116 casesJ S Waye, B Eng, M Patterson, et al.
Pageof 10